Beruflich Dokumente
Kultur Dokumente
Operation Manual
This manual may not, in whole or in part, be copied, photocopied, reproduced, translated, or converted to any electronic or
machine-readable form without prior written consent of B.Braun Medical Inc.
950520 Rev F
Table of Contents
Chapter 1 INTRODUCTION.....................................................................................1-1
Warranty ..............................................................................................................1-1
Intended Use .......................................................................................................1-2
Epidural Administration ............................................................................... 1-2
Blood Infusion .............................................................................................. 1-3
q(x)o ............................................................................................................. 1-3
Index ....................................................................................................................Index-1
This warranty will not apply to any Horizon Nxt® or component thereof
which has been: (1) repaired by anyone other than an authorized B. Braun
Medical trained technician or repair facility; (2) altered in any way that, in
B. Braun Medical’s judgement, affects its stability or reliability; (3)
subjected to misuse, negligent handling, or accident; (4) used in any manner
not in accordance with the instructions furnished by B. Braun Medical in the
Operation and/or Service Manual.
This warranty extends only to the first purchaser or lessee and does not
extend to, and may not be enforced by, any other person.
Horizon Nxt®
Modular Infusion System 1-1 6/00
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Intended Use
The Horizon Nxt® is intended for use with B. Braun Medical Horizon®
I.V. sets to regulate the flow of primary and secondary fluids when positive
pressure is required. The infusion system is capable of delivering fluid from
a negative head height (when the I.V. fluid container is lower than the
pump), and provides clinically accepted volumetric accuracy for all
standard I.V. fluids, including blood, lipids and TPN.
Because some infusions require multiple flow rates during the delivery
cycle, the Horizon Nxt is equipped with two automatic multiple delivery
rate modes. The Profile Delivery mode incorporates a standard ramped
delivery regimen, and the Programmable Delivery mode can be set up to
sequentially deliver up to nine user-selected volumes of fluid each at a user-
selected rate. Both modes are designed for ease of and can be adapted to
home-care settings.
The pump is equipped with distinct audible and visual alarm signals to
indicate KVO, low battery, and actual alarm conditions.
Epidural Administration
The Horizon Nxt can be used for epidural administration of anesthetic and
analgesic drugs.
Caution: Whenever the pump is being used for epidural infusions, the
pump’s secondary infusion features should not be used.
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For epidural administration of analgesic drugs, use indwelling catheters
specifically indicated for either short-term or long-term analgesic epidural
drug delivery.
When the Horizon Nxt® is being used for epidural infusions, the source
container and administration set should be clearly differentiated from source
containers and administration sets used for other routes of infusion.
Blood Infusion
The Horizon Nxt can be used for infusion of blood and blood products. For
blood infusion, a Horizon Pump Blood Set should be used. Do not attempt
to piggyback blood. The normal saline roller clamp on the blood tubing set
must be clamped off. The high viscosity of blood will cause the saline to
infuse before the blood if both clamps are left open.
q(x)°
The Horizon Nxt can be used for the periodic infusion of antibiotics,
chemotherapy or other IV infusions according to a schedule set by the user.
Assure that there is a maintenance IV infusing in the intervals between
pump infusions.
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Chapter 2 PRODUCT DESCRIPTION
The Horizon Nxt® has been developed in reponse to the special needs of all
caregivers in the medical setting.
Operating Modes
Profile Mode - offers a tapered delivery mode for infusing TPN or other
fluids requiring ramp up and ramp down time.
Operating States
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Illustrations:
7 6 5 4 3 2 1 9 10
21
19
19 20
20
18
18
16
16 17
17
8 12
11 13 14 15
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Figure 2: Rear View
1 2
B. Braun Medical
Carrollton, TX 75006
1 2 3
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Important Keys
An understanding of the function and location of these keys will assist in the
use of the pump.
From Figure 1:
From Figure 2:
• Panel Lock Out Switch locks the keypanel to prevent tampering. The
switch can only be used while the pump is infusing.
Daisy Chaining
Caution: To daisy chain more than 5 pumps, verify that the total leakage
current as a system does not exceed 100 uA.
Battery Operation
The Horizon Nxt has been equipped with an internal, rechargeable battery
which will power the pump automatically if the plug is disconnected during
use. Battery power is provided as a back-up system only, and the length of
the battery life is affected by the rate of delivery. Whenever possible, the
pump should remain plugged into an electrical outlet. The Battery Use
indicator will be lit when the pump is operating on its battery.
The pump must remain plugged into a hospital-grade electrical outlet for at
least 24 hours to fully recharge the battery from a totally discharged
condition.
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Chapter 3 PRINCIPLES OF OPERATION
Caution: Use only with B. Braun Medical Horizon® I.V. Sets
2) Plug the pump’s power cord into a hospital-grade electrical outlet, or the
AC Receptacle on the side of another Horizon or Horizon Nxt pump.
3) Press the Power key. If the Information Screen says:
Warning: Unrestricted fluid flow may occur if the Free Flow Protector
Clip is not properly installed in the receptacle.
Note: Do not use a pump with visible damage or with bent, damaged or
missing components.
Cassette Removal
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Standard Mode
The time left, total infused, and occlusion pressure limit are shown on the
Information Screen. Monitor the infusion according to hospital policy.
After the infusion is complete, the pump will alarm and go into the KVO
state.
1) Prepare IV fluids according to the set package. Use primary sets with
check valves.
2) Connect the piggyback set to the upper injection site (the site above the
pump) on the primary set.
3) Lower the primary bag at least 8 inches.
Note: To minimize or prevent fluid flow from the primary container during
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a piggyback infusion (sympathetic flow), it may be necessary to
lower the primary bag more than 8 inches or clamp off the primary
tubing. Sympathetic flow increases significantly when the
piggyback rate is greater than 125 ml/hr, and clamping the primary
tubing is recommended at rates greater than 125 ml/hr.
When the Piggyback volume is complete, the Piggyback Rate and Volume
Displays will blank. The Primary Rate and Volume Displays will light up.
The infusion will now be delivered at the primary rate. Make sure the
primary tubing is not clamped.
Piggyback Callback
This feature causes the pump to alarm and continue the infusion at a KVO
rate after the programmed piggyback volume is infused. Piggyback
Callback must be selected in the User menu.
Note: If the ENTER key or RUN key is not pressed within 4 seconds of
entering a new rate, a series of error beeps will occur and the rate
change will be cancelled. The pump will then display the message
"Rate change aborted", and will continue to infuse at the old rate.
An intermittent alarm will continue to sound to notify the user that a
rate change has been attempted and cancelled. Pressing any key will
silence the alarm.
With Pump on Hold:
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1) Press the HOLD key.
2) Press the DATA keys to change the rate.
3) Press the RUN key to start the infusion.
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Chapter 4 MENUS
The Horizon Nxt® can be customized to fit your specific needs. The User
Menu and Alternate Menu contain options identified by each individual
hospital. The following options will always appear in one of the 2 menus.
Main Menu
Alternate Menu
Calculate BSA calculates the body surface area (BSA).
Set LCD Contrast changes the readability of the Information Screen.
Biomed Options allows access to the Biomed Menu.
Exit from Menu returns to the Information Screen.
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Change Alarm Volume:
This feature clears the Total Volume displayed on the Information Screen.
Dose Mode:
The Dose Mode is fully described in the Dose Mode Chapter.
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Occlusion Limit
This feature lets the user change the occlusion pressure limit to 75, 100, 200,
300, 400, or 500 mmHg. At rates of 400 mL/hr and higher, the pressure
setting is automatically increased to 400 mmHg. Occlusion pressure is a
threshold value.
For Example: If the occlusion pressure is set to 300 mmHg, the pump will
infuse at the lowest pressure possible but will alarm if the
pressure required to infuse the IV fluid rises above the 300
mmHg value.
A gravity infusion of D5W with the IV container 3 feet above the IV site is
equivalent to approximately 70 mmHg.
Caution: The higher the pressure limit, the less sensitive the pump is to
changes in fluid resistance which may be caused by positional
IV’s or infiltrations. High pressure limits can increase the
severity of an infiltration without an alarm condition.
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Alternate Menu Items:
Calculate BSA:
This option allows the user to change the readability of the Information
Screen.
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Chapter 5 CUSTOM MENU OPTIONS
Each of the above options are described more fully in this chapter.
The options are listed in alphabetical order.
Discharging:
DISCHARGING
EXIT
Charging:
CHARGING
Fully Charged:
FULLY CHARGED
EXIT
The normal Hold Time is 3 minutes. Use this option to extend that
time to a maximum of 120 minutes.
"Hold" is displayed on the LEDs. Press the RUN key to cancel the
pause and begin infusing. Press the ENTER key to cancel the
extended pause and return to the standard 3 minute hold. Press the
MENU key to cancel the pause and access the Menu system.
Note: If the pump is turned on with the Micro Rate Limit activated,
a Teddy Bear shows on the LCD screen for 4 seconds.
Note: If a rate exists or is entered that is higher than the Rate Limit
set, an audible signal occurs. The user will need to lower the
rate or exit this feature.
Monitor Docking
Set-up
Occlusion Warning
PROFILE Mode
PROGRAM Mode
q(x)° Schedule
Cancel OK
To Enter Data:
VALIDATE
Note: After pressing Enter, the pump goes into a waiting period.
"SCHd dLY" shows on the LED’s. No fluid is infusing
during this period.
At the q(x)° Start time, the pump will begin the infusion. During the
infusion "SCHd run" shows on the LED’s. The number of doses
remaining is shown on the LCD. After the infusion is complete, the
pump will automatically return to the waiting period. The pump will
continue to "infuse and wait" for the total number of doses entered.
To Exit:
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Note: The pump must be in the Hold state.
This feature lets the user delay an infusion from Standard, DOSE,
PROFILE or PROGRAM Mode for up to 24 hours.
Either:
or
When the Horizon Nxt with MedScan is being used for epidural
infusions, the source container and administration set should be
clearly differentiated from source containers and administration sets
used for other routes of infusion.
Caution: The higher the pressure limit, the less sensitive the pump
is to changes in fluid resistance which may be caused by
positional IV’s or infiltrations. High pressure limits can
increase the severity of an infiltration without an alarm
condition.
Note: Data is shown from right to left. The word "Now" reinforces
the most current data is represented on the right side of the
graph. The arrow’s position, whether pointing upward or
downward, indicates either an increase or a decrease in the
downstream fluid resistance.
Note: MAX is the default setting. MIN displays more data points
compressed along the horizontal axis for a representation of a long-
term trend. MAX displays less data points in the same area for a
short-term trend.
To Exit:
If a drug name was used the last time in DOSE Mode, the following screen
will appear on the LCD:
or
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1) Press CURSOR key to select "Clear Drug"
2) Press ENTER
3) Go to Data Screen
Note: Generic calculation can be used for drugs not appearing on the list.
Epidural Category:
Concentration Screen:
Note: No data entry can be done here. The concentration can be changed
later (See Data Screen.)
Data Screen:
Body Weight:
Calculated Parameter:
Concentration, Dose and Rate are interdependent on each other for their
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numeric values. Specifying the amount of two parameters cause the third
parameter to be calculated.
Enter Data:
Rate and Volume data is transferred to the displays. The name of the
medication and "DOSE" are shown on the Information Screen.
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1) Press the left or right CURSOR keys to DOSAGE CONC BODY
move to the appropriate parameter
2) Press the up or down CURSOR keys to mcg/kg/min mg kg
change to the correct parameters (mcg/ change move
kg/min to units/hr) Press ENTER when done
3) Press ENTER key
Titrate Rate:
The rate can be titrated while the pump is running. Press the DATA keys to
change the rate. The dose is recalculated and shown. The ENTER key or RUN
key must be pressed within four seconds to validate the change. Once made,
the pump infuses at the new rate.
Note: If the ENTER key or RUN key is not pressed within 4 seconds of
entering a new rate, a series of error beeps will occur and the rate
change will be cancelled. The pump will then display the message
"Rate change aborted", and will continue to infuse at the old rate.
An intermittent alarm will continue to sound to notify the user that a
rate change has been attempted and cancelled. Pressing any key will
silence the alarm.
Titrate Dose:
Monitor the infusion as indicated by hospital policy. The pump will alarm
and go into the KVO state when the volume is infused. “KVO: DOSE
COMPLETE” is shown on the Information Screen.
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Chapter 7 SPECIAL MODES
PROFILE Mode
This mode lets the user deliver fluid in a ramped delivery pattern (ramp up,
plateau deliver, and ramp down) over a selected period of time.
If the pump was turned off while in the PROFILE Mode, the following
screen will appear:
Note: The minimum ramp time is 10 minutes; the maximum ramp time 120
minutes. The largest value for maximum rate is 400 ml/hr.
Data Entry:
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“Profile Ready” will appear at top of Information Screen.
Press RUN key to start. “PROFILE RAMP UP” will be displayed on the
Information Screen.
Restart PROFILE:
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PROGRAM Mode
This mode lets the user program up to nine different rates and volumes. The
pump will deliver the fluid sequentially. Fluid delivery can be customized
for each patient.
If the pump was turned off while in the PROGRAM Mode, this screen will
appear:
Data Entry:
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NOT ALLOWED Pd. Rate Volume
1 50.0 35.0
2 35.0 0.0
3 30.0 500.0 ZERO
VALIDATE TOTAL = 0.0 ml
ALLOWED
Pd. Rate Volume
1 50.0 35.0
2 100.0 500.0
3 0.0 0.0 ZERO
VALIDATE TOTAL = 0.0 ml
Each period is represented by a vertical bar which fills as the fluid is infused.
The height of the bar represents the rate of infusion in that particular period.
The period presently being infused is displayed in the upper left corner. If
the vertical bar appears to be missing, the rate in that period is much less
compared to the other periods.
Review/Change PROGRAM:
Restart PROGRAM:
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1) Press HOLD key
2) Press the MENU key
3) Press CURSOR keys to select “Restart PROGRAM”
4) Press ENTER key
Upon completion of the program, the pump enters the KVO state. Press the
HOLD key
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Chapter 8 MAINTENANCE
Cleaning
Clean the pump with a soft, lint-free cloth or swab dampened with soap and
water, a general nonstaining chemical disinfectant, or alcohol (90%
concentration or less.). DO NOT use acetone solutions containing
glutaraldehyde, ammonium chlorides or abrasive cleansers on the
pump. If you feel it necessary, Betadine or Iodine solutions may be used,
but they will stain the device.
Caution: To avoid electrical shock, turn off the pump and disconnect it
from the electrical outlet before cleaning.
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Alarm Procedures
An alarm notifies the user that the condition indicated on the Information
Display has occurred and that corrective action must be taken to continue
the infusion process.
1) Operation alarms - Press the MENU key to see the Help Screen which
contains the guidelines in the “Correction” column of the Alarm
Troubleshooting Guide. Clear the alarm by pressing the HOLD key.
2) System alarm - Press the HOLD key, and press the RUN key to restart the
infusion.
3) Repair Instrument alarm - Press the HOLD key and turn the pump off and
then on again (Similiar to rebooting a personal computer.). If the alarm
recurs, return the pump to a Biomedical Professionial for service.
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Alarm Troubleshooting Guide
System Error SYS Err Turn the pump off and return to Bio-
medical Professional for service
See Help SEE HELP CLOSE ROLLER CLAMP, then
open door. Press LOAD and reload
tubing.
Cassette not in place
Set Piggyback Rate Set a Piggyback rate
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Set Piggyback Volume Set a Piggyback volume
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Cautions
Before using the pump in a clinical setting, the user should become
thoroughly familiar with the proper use of the device as outlined in this
Operation Manual.
The Horizon Nxt® Infusion Pump is not intended to substitute for regular
patient observation and evaluation.
Do not attempt to infuse two fluids simultaneously using the Horizon Nxt
Infusion Pump.
Each time the pump is turned on, verify that the alarm sounds during the
momentary test sequence. If the alarm continues to sound or an alarm
message is displayed, refer to Alarm Procedures.
Unrestricted fluid flow may occur if the I.V. set is not properly installed.
Whenever the pump is being used for epidural infusion, the pumps’
secondary infusion features should not be used.
It is not recommended to stack more than five pumps on one I.V. pole.
The higher the maximum pressure limit, the less sensitive the pump is to
changes in fluid resistance which may be caused by positional I.V.'s or
infiltrations. High pressure limits can increase the severity of an infiltration
without causing an alarm condition.
To avoid electrical shock, turn off the pump and disconnect it from the
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electrical outlet before cleaning.
Do not use the pump in the presence of strong electromagnetic fields. The
field may permanently damage the pump. For further information, consult
the manufacturer of the equipment in question.
A possible electrical shock hazard exists if the case of the pump is opened
or removed. Refer all servicing to authorized service personnel.
Do not use visibly damaged pumps or pumps with bent, damaged or missing
components.
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Service and Performance Information
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Specifications
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Alarms: Air-In-Line, Container Empty, Door Open,
Downstream Occlusion, Hold Time Exceeded,
Low Battery, Low Flow from Container, Close
Roller Clamp, Sys Err, Upstream Occlusion
Air-in-Line Alarm: 0.09 cc
Hold Time Exceeded Alarm: Activated after three minutes on hold without
user interaction (deactivated if the door of the
pump is open)
Memory: Permanent data retention after the pump is
turned off, unless the battery is depleted or dis-
connected, or unless the Data Retention De-
faults have been otherwise selected in the
Biomed Options.
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Chapter 9 Table 1
Drug List
Name Concentration Dosage Units
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Name Concentration Dosage Units
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Name Concentration Dosage Units
Hydromorphone 50 mg in 5 ml mg/hr
500 mg in 50 ml
0 mg in 0 ml
Insulin (Regular) 0 units in 0 ml units/hr
0 units in 0 ml
0 units in 0 ml
Isoproterenol 3 mg in 250 ml mcg/min
6 mg in 250 ml
0 mg in 0 ml
KCL 20 mEq in 50 ml mEq/hr
40 mEq in 100 ml
0 mEq in 0 ml
Labetalol 200 mg in 200 ml mg/min
200 mg in 250 ml
0 mg in 0 ml
Lidocaine 2 gm in 500 ml mg/min
4 gm in 500 ml
0 gm in 0 ml
Magnesium Sulfate 5000 mg in 250 ml g/hr
5000 mg in 500 ml
0 mg in 0 ml
Methotrexate 0 mg in 0 ml mg/kg/min
0 mg in 0 ml
0 mg in 0 ml
Midazolam 25 mg in 50 ml mg/hr
50 mg in 50 ml
0 mg in 0 ml
Milrinone 10 mg in 10 ml mcg/kg/min
20 mg in 100 ml
0 mg in 0 ml
Morphine 10 mg in 50 ml mg/hr
10 mg in 1 ml
0 mg in 0 ml
NTG (mcg/min) 50 mg in 250 ml mcg/min
100 mg in 250 ml
0 mg in 0 ml
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Name Concentration Dosage Units
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Name Concentration Dosage Units
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Name Concentration Dosage Units
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INDEX
A
Air-In-Line, 2-3
Alarm Procedure, 8-2
Alarm Volume, 4-1, 4-2
Alternate Menu, 4-1
B
Battery Operation, 2-4
Blood Infusion, 1-3
Body Surface Area (BSA), 4-1, 4-4
C
Calculate BSA, 4-1, 4-4
Cassette Alignment Pins, 2-3
Cassette Removal, 3-1
Change Alarm Volume, 4-1, 4-2
Changing the Rate, 3-3
Check Battery Level, 5-1, 5-2
Clear Total Infused, 4-1, 4-2
D
Daisy Chaining, 2-4
Data Keys, 2-2, 2-4
Dose Mode, 2-1, 4-1, 6-1
Body Weight, 6-2
Calculated Parameter, 6-2
Change Medication, 6-1
Change SETUP Parameters, 6-3
Clear Medication, 6-1
Concentration Screen, 6-2
Data Screen, 6-2
Drug Menus, 6-1
Enter Data, 6-3
Epidural, 6-2
Exit Dose Mode, 6-4
Titrate Dose, 6-4
Titrate Rate, 6-4
E
Enter Key, 2-2, 2-4
Epidural Administration, 1-2, 5-9, 6-2
F
Free Flow Protection Clip, 2-3
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H
Hold Extender, 5-1, 5-3
I
Illustrations
Front View, 2-2
Rear View, 2-3
Inside the Door, 2-3
K
KVO, 2-1
L
LCD Contrast, 4-1, 4-4
M
Menu Key, 2-2, 2-4
Micro Rate / Limit, 5-1, 5-3
Monitor Docking, 5-4
O
Occlusion limit, 4-1, 4-3
Occlusion Warning Notification, 5-1, 5-4
P
Panel Lockout Switch, 2-3
Piggyback Callback, 3-3, 5-1, 5-5
Piggyback Fluids, 3-2
Piggyback Indicator Key, 2-2
Power Key, 2-2, 2-4
Profile Mode, 5-1, 7-1
Change Profile Parameters, 7-1
Data Entry, 7-1
Exit PROFILE Mode, 7-3
Immediate Ramp Down, 7-2
Restart PROFILE, 7-2
Review/Change PROFILE Data, 7-2
Set Profile Parameters, 7-1
Program Mode 5-1, 7-4
Data Entry, 7-4
Exit PROGRAM Mode, 7-6
Restart PROGRAM, 7-6
Review/Change PROGRAM, 7-5
Skip PROGRAM Periods, 7-6
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Q
q(x)° Schedule, 5-1, 5-5
S
Schedule Next Run, 5-1, 5-9
Select MAX Pressure, 5-1, 5-10
Set Time & Volume, 5-1, 5-11
Site Trend, 5-1, 5-12
Standard Mode, 2-1
For Primary Fluids, 3-2
For Piggyback Fluids, 3-2
Sympathetic flow, 3-3
T
Titration, 3-3, 6-4
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